A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3639164



Internal ID7025947
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:77210206..77215925hg38UCSC Ensembl
Innerchr16:77210233..77215898hg38UCSC Ensembl
Outerchr16:77210179..77215952hg38UCSC Ensembl
chr16:77244103..77249822hg19UCSC Ensembl
Innerchr16:77244130..77249795hg19UCSC Ensembl
Outerchr16:77244076..77249849hg19UCSC Ensembl
Cytoband16q23.1
Allele length
AssemblyAllele length
hg385720
hg195720
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15528312, essv15528311
SamplesNA20878, NA21100
Known GenesSYCE1L
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3639164
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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